1,3-Bis(2,6-diisopropylphenyl)imidazolium Chloride丨CAS 250285-32-6

1,3-Bis(2,6-diisopropylphenyl)imidazolium Chloride丨CAS 250285-32-6
Product Introduction:
Catalog No.: SS095805
CAS No.: 250285-32-6
Purity: 98%min
Product Name: 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride
Molecular Formula: C27H37ClN2
Molecular Weight: 425.05
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Technical Parameters
Description

Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of 1,3-bis(2,6-diisopropylphenyl)imidazolium chloride丨cas 250285-32-6 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.

 

Specifications

 

Appearance Off-white solid
Purity 98% min.

 

Transport Information

 

Parameter

Specification

UN Number

2811

Class

6.1

Packing Group

II

H.S. Code

2933290090302

Stability & Reactivity

The product is chemically stable under standard ambient conditions.

Storage

Keep container tightly closed in a dry and well-ventilated place.

Condition to Avoid

 

Package

 

 

 

 

Applications

 

1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride is an important organic salt primarily recognized as a precursor for N-heterocyclic carbene (NHC) ligands. It is widely used in organometallic and coordination chemistry, particularly as a stable source of free carbenes that can bind to transition metals. These metal–NHC complexes are valuable in catalysis, playing crucial roles in cross-coupling reactions, olefin metathesis, hydrogenation, and other catalytic transformations in fine chemical and pharmaceutical synthesis. Beyond catalysis, it serves as a versatile building block in the development of functional materials, ionic liquids, and supramolecular assemblies, owing to its thermal stability and tunable steric and electronic properties. Its use is also prominent in academic and industrial research settings, where it facilitates the design of novel metal complexes with enhanced reactivity, stability, and selectivity.

 

Benefits

 

The benefits of this compound stem from its unique steric protection and electronic characteristics provided by the bulky 2,6-diisopropylphenyl substituents. These features significantly enhance the stability of the corresponding carbene, leading to more robust and long-lived metal complexes. Such stability translates into higher efficiency and reliability in catalytic processes, reducing the need for excessive catalyst loading and lowering production costs. The compound's versatility also supports broad customization in ligand design, allowing chemists to fine-tune catalytic properties for specific transformations. In addition, its role in creating ionic liquids and functional materials contributes to advancements in green chemistry, materials science, and energy-related applications. The balance between reactivity and stability makes it an ideal choice for both fundamental research and industrial-scale processes, delivering consistent performance and expanding the range of achievable chemical transformations.

 

Conclusion

 

Overall, 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride is a highly valuable compound in modern chemistry, particularly in the preparation of NHC ligands and advanced catalytic systems. Its ability to stabilize reactive species while enabling efficient transformations provides significant benefits to both industrial and academic applications. By facilitating innovative approaches in catalysis, materials development, and molecular design, it continues to serve as a cornerstone for progress in synthetic and applied chemistry.

 

 

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